Other Names for this Disease
- Acquired haemophilia
- Hemophilia, acquired
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hemophilia in which the body makes specialized proteins called autoantibodies that attack and disable coagulation factors (proteins in the blood that assist with the clotting process). The most common coagulation factor attacked is coagulation factor VIII, though other coagulation factors, including factor V and factor IX have been associated with the condition. The production of autoantibodies is sometimes associated with pregnancy, immune system disorders (e.g., systemic lupus erythematosus, rheumatoid arthritis, Sjogren syndrome), viral infections cancer, or allergic reactions to certain drugs. In about half of cases, the cause of acquired hemophilia is unknown. Treatment may vary from person to person.Acquired hemophilia is a rare form of
Last updated: 12/5/2008
- Hemophilia. Genetics Home Reference. May 2010; http://ghr.nlm.nih.gov/condition=hemophilia. Accessed 6/16/2011.
- Zeitler H, Ulrich-Merzenich G, Hess L, Konsek E, Unkrig C, Walger P, et al. Blood. 2005; http://bloodjournal.hematologylibrary.org/cgi/reprint/105/6/2287. Accessed 10/14/2008.
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- Genetics Home Reference (GHR) contains information on Acquired hemophilia. This website is maintained by the National Library of Medicine.
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- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Acquired hemophilia. Click on the link to view a sample search on this topic.